Formation and characterization of Co(III)-semiquinonate phenoxyl radical species

Yuichi Shimazaki, Ryota Kabe, Stefan Huth, Fumito Tani, Yoshinori Naruta, Osamu Yamauchi

研究成果: ジャーナルへの寄稿学術誌査読

26 被引用数 (Scopus)


Co(III) complexes of N 3O-donor tripodal ligands, 2,4-di(tert-butyl)-6-{[bis(2-pyridyl)methyl]aminomethyl}phenolate (tbuL), 2,4-di(tert-butyl)-6-{[bis(6-methyl-2-pyridyl)methyl]aminomethyl}phenolate (tbuL(Mepy) 2), were prepared, and precursor Co(II) complexes, [Co(tbuL)CI] (1) and [Co(tbuL(Mepy) 2)Cl] (2), and ternary Co(III) complexes, [Co(tbuL)-(acac)]ClO 4 (3), [Co(tbuL)(tbu-cat)] (4), and [Co(tbuL(Mepy) 2)(tbu-SQ)]ClO 4 (5), where acac, tbu-cat, and tbu-SQ refer to pentane-2,4-dionate, 3,5-di(tert-butyl)catecholate, and 3,5-di(tert-butyl)semiquinonate, respectively, were structurally characterized by the X-ray diffraction method. Complexes 3 and 5 have a mononuclear structure with a fac-N 3O 3 donor set, while 4 has a mer-N 3O 3 structure. The cyclic voltammogram (CV) of complex 3 exhibited one reversible redox wave centered at 0.93 V (vs Ag/AgCl) in CH 3CN. Complex 5 was converted to a phenoxyl radical species upon oxidation with Ce(IV), showing a characteristic π-π* transition band at 412 nm. The ESR spectrum at low temperature and the resonance Raman spectrum of 3 established that the radical species has a Co(III)-phenoxyl radical bond. On the other hand, the CVs showed two oxidation processes at E 1/2 = 0.01 and E pa = 0.92 V for 4 and E 1/2a = 0.05 and E 1/2b = 0.69 V for 5. The rest potential of 4 (-0.11 V) was lower than the E 1/2 value, whereas that of 5 (0.18 V) was higher, indicating that the first redox wave of 4 and 5 is assigned to the tbu-cat and the tbu-SQ redox process, respectively. One-electron oxidized 4 showed absorption, resonance Raman, and ESR spectra which are similar to those of 5, suggesting formation of a stable Co(III)-semiquinonate species, which has the same oxidation level of 5. The resonance Raman spectrum of two-electron oxidized 4 showed the ν 8a bands of the semiquinonate and phenoxyl radical, which were absent in the spectrum of one-electron oxidized 5. Since both oxidized species were ESR inactive at 5 K, the former was concluded to be a biradical species containing semiquinonate and phenoxyl radicals coupled antiferromagnetically and the latter to a species with a coordinated quinone.

ジャーナルInorganic chemistry
出版ステータス出版済み - 7月 23 2007

!!!All Science Journal Classification (ASJC) codes

  • 物理化学および理論化学
  • 無機化学


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